Preface |
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xxi | |
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Part 1 Introduction to the Fundamentals |
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1 | (78) |
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1 Lipid-Based Nanocarriers as Drug Delivery System and Its Applications |
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3 | (28) |
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3 | (1) |
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4 | (1) |
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1.2 An Overview on Nanocarriers |
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5 | (1) |
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1.3 Types of Nanocarriers |
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6 | (6) |
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6 | (1) |
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1.3.2 Solid Lipid Nanoparticles |
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7 | (1) |
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1.3.3 Nanostructured Lipid Carriers System |
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7 | (2) |
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9 | (1) |
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1.3.5 SMEDDS, SEDDS, and SNEDDS |
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9 | (1) |
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1.3.6 Crystalline Mesophases |
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10 | (2) |
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1.4 Methods of Preparation of Lipid Nanocarriers |
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12 | (1) |
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1.5 Challenges and Hurdles |
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12 | (2) |
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1.5.1 Scale Up and Stability Issues |
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12 | (2) |
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1.5.2 In Vivo Elimination of Nanocarriers |
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14 | (1) |
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1.6 Characterization Techniques for Lipid Nanocarriers |
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14 | (3) |
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1.6.1 Size and Morphology |
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14 | (1) |
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15 | (1) |
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16 | (1) |
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16 | (1) |
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1.6.5 Spectroscopic Analysis |
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16 | (1) |
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1.7 Application of Lipid-Based Nanocarriers |
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17 | (2) |
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1.7.1 Application in Drug Delivery |
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17 | (1) |
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1.7.2 Application in Therapeutic Nucleic Acid Delivery |
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18 | (1) |
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1.7.3 Application in Delivery of Peptide/Hormone |
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19 | (1) |
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19 | (1) |
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20 | (11) |
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2 Nanoparticulate Carriers--Versatile Delivery Systems |
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31 | (24) |
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31 | (1) |
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32 | (1) |
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2.2 Classification of Nanoparticulate Carriers |
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33 | (10) |
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2.2.1 Lipid-Based Nanocarriers |
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33 | (4) |
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2.2.1.1 Ph-Sensitive Lipid Carriers |
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37 | (1) |
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2.2.1.2 Thermo-Responsive Lipid Carriers |
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38 | (1) |
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39 | (1) |
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39 | (1) |
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2.2.3.1 Gold Nanoparticles (AuNPs) |
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39 | (1) |
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2.2.3.2 Iron Oxide Nanoparticles |
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40 | (1) |
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40 | (1) |
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2.2.4 Self-Emulsifying Drug Delivery Systems (SEDDS) |
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41 | (1) |
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2.2.5 Polymer-Based Nanoparticles |
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41 | (2) |
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2.3 Various Applications of Nanoparticulate Carriers |
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43 | (2) |
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2.3.1 Tissue Engineering and Regenerative Medicine |
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43 | (1) |
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2.3.2 Delivery of Proteins |
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44 | (1) |
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2.3.3 Delivery of Vaccines |
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44 | (1) |
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44 | (1) |
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2.3.5 Phagokinetic Studies |
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45 | (1) |
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2.4 Modes of Transport of Nanoparticulate Carriers |
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45 | (3) |
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48 | (1) |
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48 | (7) |
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3 Nanotools in Customized Drug Delivery System |
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55 | (24) |
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K. J. Thirumalai Subramaniam |
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Veera Venkata Satyanarayana Reddy Karri |
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55 | (1) |
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56 | (1) |
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3.2 Concept of Personalized Medicines |
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57 | (3) |
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3.3 Customized Nanotools and Their Benefits |
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60 | (10) |
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64 | (1) |
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3.3.2 Solid Lipid Nanoparticles (SLNs) |
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65 | (1) |
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66 | (1) |
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3.3.4 Polymer-Based Nanoparticles |
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66 | (1) |
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3.3.5 Polymer-Based Micelles |
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66 | (1) |
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67 | (1) |
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3.3.7 Metallic Nanoparticles |
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68 | (1) |
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3.3.7.1 Gold Nanoparticles |
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68 | (1) |
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3.3.7.2 Iron Oxide Nanoparticles |
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69 | (1) |
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69 | (1) |
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69 | (1) |
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3.4 Applications of Nanotechnology in Personalized Medicine |
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70 | (3) |
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73 | (1) |
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74 | (1) |
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74 | (5) |
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Part 2 Novel and Modernized Nanoscale Delivery Systems: Revolutionary Progress in the Field of Pharmacy |
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79 | (254) |
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4 Dendrimers: Role in Novel Drug Delivery |
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81 | (18) |
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81 | (1) |
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81 | (2) |
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4.1.1 Advantages of Dendrimers |
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82 | (1) |
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4.1.2 Role of Dendrimers in Drug Delivery |
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82 | (1) |
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4.2 Components of Dendrimers |
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83 | (1) |
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4.3 Synthesis of Dendrimers |
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84 | (1) |
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4.4 Classification of Dendrimers |
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84 | (4) |
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4.4.1 Hydrophilic Dendrimers |
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85 | (1) |
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4.4.2 Biodegradable Dendrimers |
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85 | (1) |
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4.4.3 Dendrimers with Amino Acids |
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85 | (1) |
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86 | (1) |
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4.4.5 Hydrophobic Dendrimers |
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86 | (1) |
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4.4.6 Asymmetric Dendrimers |
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86 | (1) |
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86 | (1) |
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4.4.8 Liquid Crystalline Dendrimers |
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87 | (1) |
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87 | (1) |
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4.4.10 Micellar Dendrimers |
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87 | (1) |
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87 | (1) |
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4.4.12 Amphiphilic Dendrimers |
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87 | (1) |
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87 | (1) |
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87 | (1) |
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4.4.15 Multilingual Dendrimers |
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88 | (1) |
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4.4.16 Multiple Antigen Peptide Dendrimers |
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88 | (1) |
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4.5 Properties of Dendrimers |
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88 | (1) |
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4.6 Mechanism of Drug Entrapment in Dendrimers |
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89 | (2) |
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4.6.1 Physical Encapsulation of the Drugs |
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90 | (1) |
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4.6.2 Electrostatic Interactions |
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90 | (1) |
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4.6.3 Covalent Conjugations |
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90 | (1) |
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4.7 Dendrimers as Delivery Agents |
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91 | (3) |
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4.7.1 Dendrimers as Oral Drug Delivery System |
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91 | (2) |
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4.7.2 Dendrimers in Nasal Drug Delivery |
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93 | (1) |
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4.7.3 Dendrimers as Carriers for Anticancer Treatment and Diagnosis |
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93 | (1) |
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4.7.3.1 Dendrimers as Carriers for Anticancer Drugs |
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93 | (1) |
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4.7.3.2 Dendrimers as Diagnostic Agents Cancer |
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94 | (1) |
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94 | (1) |
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95 | (4) |
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5 Nanofibers in Drug Delivery |
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99 | (26) |
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99 | (2) |
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101 | (8) |
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5.2 Nanofiber as Oral Drug Delivery System |
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109 | (1) |
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5.3 Nanofiber as Topical Drug Delivery System |
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110 | (2) |
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5.4 Nanofiber as Parenteral Drug Delivery System |
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112 | (1) |
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5.5 Nanofiber as Multimodal Drug Delivery System |
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112 | (6) |
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5.5.1 Cardiovascular Disorder |
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112 | (1) |
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113 | (1) |
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113 | (1) |
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113 | (1) |
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114 | (1) |
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5.5.6 Antimicrobial Therapy |
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114 | (1) |
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115 | (1) |
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116 | (1) |
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117 | (1) |
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117 | (1) |
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5.6 Challenges and Future Perspective |
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118 | (1) |
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118 | (1) |
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118 | (7) |
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6 Microbubbles used for Drug Delivery System |
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125 | (20) |
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125 | (1) |
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126 | (1) |
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6.2 Structural Components of Microbubble |
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127 | (3) |
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128 | (1) |
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128 | (1) |
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128 | (1) |
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6.2.2.2 Surfactant Shells |
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128 | (1) |
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128 | (1) |
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129 | (1) |
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6.3 Methods of Preparation Microbubbles |
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130 | (2) |
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6.3.1 Sonication Technique |
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130 | (1) |
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6.3.2 Cross-Linked Polymer Technique |
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130 | (1) |
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6.3.3 Emulsion Solvent Evaporation Technique |
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131 | (1) |
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6.3.4 Atomization and Reconstitution Technique |
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132 | (1) |
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6.4 Acoustic Nature of Microbubble |
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132 | (1) |
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6.4.1 Response Under Low Frequency |
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132 | (1) |
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6.4.2 Response Under High Frequency |
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133 | (1) |
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6.5 Characterizations of Microbubbles |
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133 | (2) |
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6.5.1 Determination of Bubble Size |
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133 | (1) |
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6.5.2 Determination of Bubble Densities |
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134 | (1) |
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6.5.3 In Vitro Floating Properties |
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134 | (1) |
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6.5.4 Microscope Observation and Diameter Measurement |
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135 | (1) |
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6.5.5 MB Diameter Measurement |
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135 | (1) |
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6.5.6 MB Concentration Determination |
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135 | (1) |
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6.5.7 Acoustic Stability of MBs |
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135 | (1) |
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6.6 Applications of Microbubbles |
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135 | (4) |
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6.6.1 Diagnostic Applications of Microbubble |
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136 | (1) |
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6.6.2 Therapeutic Potential of Microbubbles |
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137 | (2) |
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6.7 Conclusions and Future Prospective |
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139 | (1) |
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139 | (6) |
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7 Virosomes: A Viral Envelope System Having a Promising Application in Vaccination and Drug Delivery System |
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145 | (16) |
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145 | (1) |
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146 | (1) |
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147 | (1) |
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7.3 Comparison of Virosomes With Liposomes |
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148 | (1) |
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7.4 Methods of Preparation of Virosomes |
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148 | (1) |
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148 | (1) |
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7.4.2 Selection of Compound of Interest (Antigen/Drug/Macromolecule) |
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149 | (1) |
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7.4.3 Membrane Reconstitution |
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149 | (1) |
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7.5 Characterization of Virosomes |
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149 | (1) |
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7.6 Applications of Virosomal Technology |
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150 | (7) |
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7.6.1 Virosomes for Vaccination |
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151 | (1) |
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7.6.1.1 Virosomes for Antigen Delivery |
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151 | (1) |
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7.6.1.2 Virosomes as Adjuvants in Human Vaccine Formulations |
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152 | (1) |
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7.6.1.3 Virosomes Complexed With Adjuvants |
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153 | (1) |
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7.6.1.4 Some Commercial Virosome-Based Vaccines |
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154 | (1) |
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7.6.2 Virosomes for Drug Delivery |
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154 | (1) |
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7.6.3 Virosomes for Cancer Immunotherapy |
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155 | (2) |
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157 | (1) |
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157 | (4) |
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8 Nanocarriers: A Tool for Effective Gene Delivery |
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161 | (26) |
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161 | (1) |
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162 | (1) |
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8.2 Key Steps in Gene Delivery |
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163 | (1) |
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8.3 Success and Existing Challenges for Gene Delivery |
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163 | (1) |
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8.4 In Vitro and In Vivo Barriers Towards Successful Gene Transfer |
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164 | (1) |
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8.5 Genetic Material That can be Delivered in Gene Therapy |
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165 | (1) |
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8.6 Role of Nanocarriers in a Nucleic Acid Delivery |
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165 | (1) |
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8.7 Nanocarriers used for Delivering Gene |
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166 | (9) |
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8.7.1 Polymeric Nanocarriers |
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166 | (1) |
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166 | (3) |
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8.7.3 Protein Nanocarriers for Gene Delivery |
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169 | (1) |
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8.7.4 Magnetic Nanocarriers |
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170 | (1) |
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171 | (1) |
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172 | (1) |
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172 | (1) |
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8.7.8 Stimuli Responsive Nanocarriers |
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173 | (1) |
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8.7.9 Ph Sensitive Liposomes |
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174 | (1) |
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8.7.10 Temperature Responsive Nanocarriers |
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174 | (1) |
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8.7.11 Redox Sensitive Nanocarriers |
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175 | (1) |
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8.8 Cellular Uptake of Nanocarriers and Their Fate Inside the Cell |
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175 | (1) |
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8.8.1 Cellular Uptake and Intracellular Trafficking of NPs |
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175 | (1) |
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8.9 Physicochemical Properties of Nanoparticles Affecting Their Uptake |
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176 | (1) |
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8.10 Targeted Delivery of Genes Using Nanocarriers |
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177 | (1) |
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177 | (1) |
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178 | (2) |
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8.13 Diseases Cured by Gene Therapy |
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180 | (1) |
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180 | (1) |
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8.15 Current Trends and Approved Products |
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180 | (3) |
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183 | (1) |
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183 | (4) |
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9 Phytosomes--Nanoarchitectures' Promising Clinical Applications and Therapeutics |
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187 | (30) |
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187 | (1) |
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188 | (1) |
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189 | (1) |
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9.2 Structure of Phytosomes |
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189 | (1) |
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9.3 Components of Phytosomes |
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190 | (2) |
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9.3.1 Phyto-Active Ingredients |
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190 | (1) |
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191 | (1) |
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9.3.3 Stoichiometric Ratio of Phospholipids and Active Phyto-Constituents |
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191 | (1) |
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192 | (1) |
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9.4 Synthesis of Phytosomes |
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192 | (1) |
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192 | (1) |
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9.5 Characterization of Phytosomes |
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193 | (3) |
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9.5.1 Morphological Visualization |
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193 | (1) |
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9.5.2 Stability of Vesicles |
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193 | (1) |
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9.5.3 Zeta Potential and Vesicle Size |
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194 | (1) |
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9.5.4 Transition Temperature |
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194 | (1) |
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194 | (1) |
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9.5.6 Entrapment Efficiency |
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195 | (1) |
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9.5.7 Partition Co-Efficient and Solubility |
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195 | (1) |
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9.5.8 Spectroscopic Approaches |
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195 | (1) |
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9.5.8.1 Fourier Transform Infrared Spectroscopy (FTIR) |
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195 | (1) |
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9.5.8.2 Nuclear Magnetic Resonance (NMR) |
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195 | (1) |
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9.6 Absorption Mechanism of Phytosomes |
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196 | (1) |
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9.7 Applications of Phytosomes |
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196 | (4) |
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9.7.1 Phytosomes in Cancer Therapy |
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197 | (1) |
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9.7.2 Phytosomes in Diabetes |
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198 | (1) |
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9.7.3 Phytosomes in Brain Delivery |
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199 | (1) |
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9.7.4 Phytosomes in Wound Healing |
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199 | (1) |
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9.7.5 Phytosomes in Liver Diseases |
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200 | (1) |
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9.8 Recent Trends and Advancements in Phytosomal Delivery |
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200 | (8) |
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208 | (1) |
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209 | (1) |
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210 | (7) |
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10 Saponin Stabilized Emulsion as Sustainable Drug Delivery System: Current Status and Future Prospects |
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217 | (20) |
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217 | (1) |
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218 | (1) |
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10.2 Saponins as Surfactant |
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219 | (10) |
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10.2.1 Quillaja saponaria |
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219 | (4) |
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10.2.2 Sapindus mukorossi |
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223 | (1) |
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10.2.3 Glycyrrhiza glabra |
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224 | (1) |
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225 | (1) |
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226 | (1) |
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10.2.6 Aesculus hippocastanum |
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227 | (1) |
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227 | (1) |
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228 | (1) |
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10.2.9 Saponaria officinalis |
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228 | (1) |
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10.3 Pharmaceutical Advantages |
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229 | (1) |
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10.4 Conclusion and Future Prospects |
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230 | (1) |
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231 | (6) |
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11 Mono and Multi-Stimuli Responsive Polymers: Application as Intelligent Nano-Drug Delivery Systems |
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237 | (30) |
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Panchaxari Mallappa Dandagi |
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237 | (1) |
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238 | (2) |
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11.2 Smart or Stimuli-Responsive Polymers for Drug Delivery |
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240 | (11) |
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11.2.1 Mono-Stimuli Responsive Polymers |
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240 | (1) |
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11.2.2 Dual-Stimuli Responsive Polymers |
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240 | (1) |
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11.2.3 Multi-Responsive Polymers |
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240 | (1) |
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11.2.4 Ph Responsive Polymers and Delivery Systems |
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240 | (4) |
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11.2.5 Temperature Responsive Polymers in Drug Delivery |
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244 | (1) |
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11.2.6 Light Responsive Drug Delivery Systems |
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245 | (3) |
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11.2.7 Magnetically Responsive Polymeric Drug Delivery Systems |
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248 | (1) |
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11.2.7.1 Static (Constant) Field Systems |
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248 | (1) |
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11.2.7.2 Varying Magnet Field Systems (VMFS) |
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249 | (1) |
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11.2.8 Other Stimuli Responsive Polymeric Nanoparticles |
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249 | (2) |
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11.3 Dual and Multi-Stimuli Responsive Drug Delivery Systems |
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251 | (6) |
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257 | (1) |
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257 | (10) |
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12 An Insight into Nanosomes: Potential Nanopharmaceutical Delivery System |
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267 | (18) |
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267 | (1) |
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268 | (3) |
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12.2 General Methods of Preparation of Nanosomes and Drug Loading |
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271 | (2) |
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12.3 Trafficking Mechanism in the Body |
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273 | (2) |
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12.4 Sterilization of Nanosomes |
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275 | (1) |
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12.5 Evaluation Parameters |
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275 | (1) |
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12.5.1 Determination of Particle Size |
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275 | (1) |
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12.5.2 Determination of Zeta Potential |
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275 | (1) |
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12.5.3 Morphological Study |
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276 | (1) |
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12.5.4 In Vitro Release Studies |
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276 | (1) |
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12.5.5 Determination of Encapsulation Efficiency |
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276 | (1) |
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276 | (1) |
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12.5.7 Stability on Storage |
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276 | (1) |
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276 | (3) |
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279 | (1) |
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279 | (6) |
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13 Nano-Structures as Bioelectronics for Controlled Drug Delivery |
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285 | (24) |
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285 | (2) |
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287 | (3) |
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13.2 Electroactive Biopolymer |
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290 | (2) |
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13.3 Electrochemical Desorption From Micro and Nanostructures of Conductive Polymers |
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292 | (3) |
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13.4 Electrochemical Desorption From Micro and Nano-Composites of Conductive Polymers |
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295 | (2) |
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13.5 Electrochemical Desorption of Self-Assembled Monolayer From a Gold Surface |
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297 | (1) |
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13.6 Electrochemically Actuated Release of Biochemicals |
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298 | (1) |
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13.7 Biochemical Release Controlled by Electrochemical Erosion of Electrolyte Hydrogel and Nanofilm |
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299 | (1) |
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13.8 Biochemical Release by Electrochemical and Electrothermal Erosion of Metallic Sealing Membranes |
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300 | (1) |
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13.9 Release of Biochemicals by Fluidic Nano-Pumps and Rotating Nano-Motors Powered by Electric Fields |
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301 | (3) |
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13.9.1 Electro-Osmotic Nano-Pumps |
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301 | (1) |
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302 | (1) |
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13.9.3 Electrically Driven Nanomotors |
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303 | (1) |
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13.10 Conclusion and Future Aspects |
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304 | (1) |
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305 | (4) |
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14 Bioadhesive Nanoparticulate Drug Delivery System |
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309 | (24) |
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Rajashree Shashidhar Masareddy |
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309 | (1) |
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310 | (1) |
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311 | (1) |
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311 | (2) |
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14.4 Theories of Mucoadhesion |
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313 | (2) |
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313 | (1) |
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314 | (1) |
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314 | (1) |
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314 | (1) |
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14.5 Mechanism of Mucoadhesion |
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315 | (1) |
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14.6 Polymers Used to Prepare Mucoadhesive Nanoparticles |
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315 | (2) |
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14.7 Ideal Properties of Mucoadhesive Polymers |
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317 | (1) |
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14.8 Mucoadhesion of Nanoparticles |
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318 | (1) |
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14.9 Preparation Methods of Mucoadhesive Polymeric Nanoparticles |
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319 | (3) |
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14.9.1 Solvent Displacement Method |
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319 | (1) |
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14.9.2 Surface Modification of Nanoparticles With Mucoadhesive Polymers |
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320 | (1) |
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14.9.3 Emulsion Polymerization |
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321 | (1) |
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14.10 Evaluation of Mucoadhesive Systems |
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322 | (3) |
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14.10.1 In Vitro and Ex Vivo Tests |
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322 | (1) |
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14.10.2 Measurement of Tensile Strength |
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323 | (1) |
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14.10.3 Measurement of Detachment Force |
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323 | (1) |
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14.10.4 Falling Liquid Film Method |
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323 | (1) |
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14.10.5 Colloidal Gold Staining Method |
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323 | (1) |
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324 | (1) |
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14.10.7 Confocal Laser Scanning Microscopic (CLSM) Method |
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324 | (1) |
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324 | (1) |
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14.10.8.1 Gamma Scintigraphy |
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324 | (1) |
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14.10.8.2 X-Ray (GI Transit Time) Studies |
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324 | (1) |
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14.10.8.3 Isolated Loop Technique |
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325 | (1) |
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14.11 Evaluation Tests of Mucoadhesive Nanoparticulate Systems |
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325 | (1) |
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325 | (1) |
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14.11.2 Atomic Force Microscopy |
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325 | (1) |
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14.11.3 Fluorophotometric Evaluation |
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326 | (1) |
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326 | (1) |
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327 | (1) |
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327 | (6) |
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Part 3 Understanding Targeted Delivery Systems |
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333 | (114) |
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15 Nanopharmaceuticals: An Approach for Effective Management of Breast Cancer |
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335 | (22) |
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335 | (1) |
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336 | (1) |
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15.2 Stages of Breast Cancer |
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337 | (1) |
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15.3 Main Types of Breast Cancer |
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337 | (1) |
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15.4 Drawbacks in Conventional Treatment |
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338 | (1) |
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15.5 Nanoparticulate Approach for Effective Management of Breast Cancer |
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339 | (2) |
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15.6 Systematic Drug Delivery System Approaches |
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341 | (3) |
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15.6.1 Metallic Nano Drug Carrier |
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341 | (1) |
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15.6.1.1 Magnetic Nanoparticles |
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341 | (1) |
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15.6.1.2 Gold Nanoparticles |
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341 | (1) |
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15.6.1.3 Superparamagnetic Iron Oxide (SPIO) |
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341 | (1) |
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15.6.2 Polymer-Based Drug Carriers |
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342 | (1) |
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15.6.2.1 Polymeric Nanoparticles |
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342 | (1) |
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15.6.2.2 Polymeric Micelles |
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342 | (1) |
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343 | (1) |
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15.6.3 Drug Carriers Based on Lipid |
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343 | (1) |
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343 | (1) |
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15.6.4 Viral Nanoparticles |
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343 | (1) |
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344 | (1) |
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15.7 Nanoparticles Targeted Drug Delivery |
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344 | (3) |
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15.7.1 Morphology of Nanoparticles |
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345 | (1) |
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345 | (1) |
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15.7.1.2 Surface Characteristics |
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345 | (1) |
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345 | (1) |
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15.7.2.1 Increase Permeability and Retention Time |
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345 | (1) |
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15.7.2.2 Tumor Physiology |
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346 | (1) |
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346 | (1) |
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15.7.3.1 Antigen or Receptor Expression |
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347 | (1) |
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15.7.3.2 Internalization of Targeted Conjugates |
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347 | (1) |
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15.8 Various Ligands used for Targeting Cancer Cells |
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347 | (2) |
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347 | (1) |
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347 | (1) |
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348 | (1) |
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348 | (1) |
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349 | (1) |
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15.8.6 Epidermal Growth Factor Receptor (EGFR) |
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349 | (1) |
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349 | (1) |
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349 | (1) |
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15.9 New Innovative Pharmaceutical Entities and Targeting Moieties |
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349 | (1) |
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15.10 Future of Cancer Treatment in Nanotechnology |
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350 | (1) |
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351 | (1) |
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351 | (6) |
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16 Vaginal Nano-Based Drug Delivery System |
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357 | (22) |
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357 | (1) |
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358 | (1) |
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16.2 Vaginal Anatomy Physiology and Diseases of Vagina |
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359 | (2) |
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16.2.1 Physiology of Vagina |
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359 | (1) |
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16.2.2 Vaginal Infections |
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360 | (1) |
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16.3 Advantages of Vaginal Drug Delivery |
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361 | (1) |
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16.4 Drawbacks of Conventional Vaginal Formulation |
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362 | (1) |
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16.5 Need of Nanocarriers for Vaginal Delivery |
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363 | (1) |
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16.6 Different Types of Nanoparticles for Vaginal Therapy |
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363 | (8) |
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16.6.1 Concept of pH-Sensitive Nanoparticles |
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364 | (1) |
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16.6.2 Acid Labile Products (Nucleic Materials/Proteins/Peptides) |
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365 | (1) |
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16.6.3 Mucoadhesive Nanoparticles |
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365 | (1) |
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16.6.4 Mucous-Penetrating Nanoparticles |
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366 | (1) |
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16.6.5 PEGylated Nanoparticles |
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366 | (1) |
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366 | (1) |
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367 | (1) |
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367 | (1) |
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367 | (1) |
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16.6.10 Metallic Nanoparticles |
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367 | (4) |
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16.6.11 Diagnostic Nanoparticles |
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371 | (1) |
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|
371 | (2) |
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16.8 Nanotoxicity: Future Prospective |
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|
373 | (1) |
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374 | (1) |
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|
374 | (5) |
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17 Recent Advances in Polymer-Modified Liposomes for Cancer Treatment |
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379 | (28) |
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379 | (1) |
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380 | (1) |
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|
380 | (21) |
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17.2.1 Structure of Liposomes |
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|
380 | (1) |
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17.2.2 Classification of Liposomes |
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|
381 | (1) |
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17.2.3 Preparation of Liposomes |
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|
381 | (1) |
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17.2.4 Drug Encapsulation Into Liposomes |
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382 | (1) |
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17.2.4.1 Active Loading of a Drug Into Liposome |
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|
382 | (1) |
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17.2.4.2 Passive Loading of a Drug Into Liposome |
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|
383 | (1) |
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17.2.5 Mechanism of Liposomes |
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|
383 | (1) |
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17.2.6 Liposomes in Cancer Treatment |
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|
384 | (1) |
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17.2.7 Liposomal Formulations Available in Clinical Trials for Cancer Treatment |
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|
384 | (4) |
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17.2.8 Liposomes Targeting Cancerous Cells |
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|
388 | (1) |
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17.2.8.1 Liposome Mediated Active Targeting of Cancer Cells |
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388 | (2) |
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17.2.8.2 Liposome Mediated Passive Targeting of Cancer Cells |
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|
390 | (1) |
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17.2.9 Strategies for Targeting Liposomes at Cancer Specific Site |
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|
391 | (1) |
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17.2.9.1 Increased Permeability & Retention (EPR) Effect and their Application in Cancer Treatment |
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|
391 | (1) |
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17.2.9.2 Surface Engineered Liposomes Mediated Active Targeting with Functionalized Targeting Ligands |
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|
392 | (1) |
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17.2.10 Approaches for Enhanced Delivery of Chemotherapeutic Drugs at Tissue Specific Site via Functionalized Liposomes Responsive Towards Stimuli |
|
|
393 | (1) |
|
17.2.10.1 Liposomes Responsive to Temperature |
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|
393 | (2) |
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17.2.10.2 Liposomes Responsive to pH |
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|
395 | (1) |
|
17.2.10.3 Liposomes Responsive to Magnetic Field |
|
|
395 | (1) |
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17.2.10.4 Liposomes Responsive to Ultrasound |
|
|
395 | (1) |
|
17.2.11 Role of Polymers in Drug Delivery for the Treatment of Cancer |
|
|
395 | (6) |
|
17.3 Future Challenges Associated With Cancer Therapy |
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|
401 | (1) |
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|
402 | (1) |
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|
402 | (5) |
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18 Role of Nanomedicines in Neglected Tropical Diseases |
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|
407 | (40) |
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|
407 | (1) |
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|
408 | (1) |
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|
409 | (23) |
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|
409 | (1) |
|
18.2.1.1 Current Therapeutics for Buruli Ulcer |
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|
410 | (1) |
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18.2.1.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Buruli Ulcer |
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|
410 | (1) |
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|
410 | (1) |
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18.2.2.1 Current Treatment for Chagas Disease |
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|
411 | (1) |
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18.2.2.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Chagas Disease |
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|
412 | (1) |
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|
413 | (1) |
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18.2.3.1 Current Treatment for Cysticercosis |
|
|
413 | (1) |
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18.2.3.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Cysticercosis |
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|
414 | (1) |
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|
414 | (1) |
|
18.2.4.1 Current Treatment for Dengue Fever |
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|
414 | (1) |
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18.2.4.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Dengue Fever |
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|
415 | (1) |
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|
415 | (1) |
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18.2.5.1 Current Treatment for Dracunculosis |
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|
415 | (1) |
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18.2.5.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Dracunculosis |
|
|
416 | (1) |
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|
416 | (1) |
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18.2.6.1 Current Treatment for Echinococcosis |
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|
416 | (1) |
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18.2.6.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Echinococcosis |
|
|
417 | (1) |
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|
417 | (1) |
|
18.2.7.1 Current Treatment for Fascioliasis |
|
|
417 | (1) |
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18.2.7.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Fascioliasis |
|
|
418 | (1) |
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18.2.8 Foodborne Trematodes |
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|
418 | (1) |
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18.2.8.1 Current Treatment for Foodborne Trematodes |
|
|
419 | (1) |
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18.2.8.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Foodborne Trematodes |
|
|
419 | (1) |
|
18.2.9 Human African Trypanosomiasis |
|
|
419 | (1) |
|
18.2.9.1 Current Treatment for Human African Trypanosomiasis |
|
|
420 | (1) |
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18.2.9.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Human African Trypanosomiasis |
|
|
420 | (1) |
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|
421 | (1) |
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18.2.10.1 Current Treatment for Leishmaniasis |
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|
421 | (1) |
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18.2.10.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Leishmaniasis |
|
|
421 | (2) |
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|
423 | (1) |
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18.2.11.1 Current Treatment for Leprosy |
|
|
423 | (1) |
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18.2.11.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Leprosy |
|
|
423 | (1) |
|
18.2.12 Lymphatic Filariasis |
|
|
424 | (1) |
|
18.2.12.1 Current Treatment for Lymphatic Filariasis |
|
|
424 | (1) |
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18.2.12.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Lymphatic Filariasis |
|
|
424 | (1) |
|
18.2.13 Mycetoma, Chromoblastomycosis and Other Deep Mycoses |
|
|
425 | (1) |
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18.2.13.1 Current Treatment for Mycetoma, Chromoblastomycosis and Other Deep Mycoses |
|
|
425 | (1) |
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18.2.13.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Mycetoma, Chromoblastomycosis and Other Deep Mycoses |
|
|
425 | (1) |
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|
425 | (2) |
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18.2.14.1 Current Treatment for Onchocerciasis |
|
|
427 | (1) |
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18.2.14.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Onchocerciasis |
|
|
427 | (1) |
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|
427 | (1) |
|
18.2.15.1 Current Treatment for Rabies |
|
|
428 | (1) |
|
18.2.15.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Rabies |
|
|
428 | (1) |
|
|
428 | (1) |
|
18.2.16.1 Current Treatment for Schistosomiasis |
|
|
428 | (1) |
|
18.2.16.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Schistosomiasis |
|
|
429 | (1) |
|
18.2.17 Snakebite Envenoming |
|
|
429 | (1) |
|
18.2.18 Soil-Transmitted Helminthiases |
|
|
430 | (1) |
|
18.2.18.1 Treatment for Soil-Transmitted Helminthiases |
|
|
430 | (1) |
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18.2.18.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Soil-Transmitted Helminthiases |
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|
430 | (1) |
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|
430 | (1) |
|
18.2.19.1 Treatment for Trachoma |
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431 | (1) |
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18.2.19.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Trachoma |
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|
431 | (1) |
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|
432 | (1) |
|
18.2.20.1 Treatment for Yaws |
|
|
432 | (1) |
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18.2.20.2 Issues in Prevailing Therapy and Status of Nanomedicine in Treatment of Yaws |
|
|
432 | (1) |
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|
432 | (5) |
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|
437 | (1) |
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|
438 | (9) |
|
Part 4 Overview of Regulatory Affairs |
|
|
447 | (26) |
|
19 Current Framework, Ethical Consideration and Future Challenges of Regulatory Approach for Nano-Based Products |
|
|
449 | (24) |
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|
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449 | (1) |
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|
450 | (1) |
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19.2 Issues in Aspect of Regulation of Drug Delivery System |
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|
451 | (1) |
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19.2.1 Environmental, Health and Safety Risks |
|
|
451 | (1) |
|
19.2.2 Ethical, Legal and Social Issues |
|
|
451 | (1) |
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19.3 Regulation of Nano-Based Products in Global Realms of the World |
|
|
452 | (6) |
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|
453 | (1) |
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19.3.1.1 Agency of US Environmental Protection |
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|
453 | (1) |
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19.3.1.2 United States of Food and Drug Administration |
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454 | (1) |
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454 | (1) |
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19.3.3 European Union (EU) |
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455 | (1) |
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19.3.3.1 Progress of Regulatory Measures in European Union |
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456 | (1) |
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457 | (1) |
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|
458 | (1) |
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|
458 | (1) |
|
19.4 Regulatory Challenges and Solutions in DDS Development |
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|
458 | (11) |
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|
467 | (1) |
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19.4.2 Chemistry, Manufacturing and Control |
|
|
467 | (1) |
|
19.4.3 Non-Clinical Safety |
|
|
468 | (1) |
|
19.4.4 Clinical Studies and Post Marketing Surveillance |
|
|
468 | (1) |
|
19.5 Regulatory Education and its Involvement in Pharmaceutical Industry for the Development of Novel Drug Delivery Systems |
|
|
469 | (1) |
|
19.6 Current Framework and Future Challenges |
|
|
469 | (1) |
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|
470 | (1) |
|
|
471 | (2) |
Index |
|
473 | |